A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869663



Internal ID6338015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97495358..97503151hg38UCSC Ensembl
Innerchr13:97495397..97503113hg38UCSC Ensembl
Outerchr13:97495320..97503190hg38UCSC Ensembl
chr13:98147612..98155405hg19UCSC Ensembl
Innerchr13:98147651..98155367hg19UCSC Ensembl
Outerchr13:98147574..98155444hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg387794
hg197794
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633294
Supporting Variants
SamplesNA19984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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